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US5695734A - Process for the separation of carbon nanotubes from graphite - Google Patents

Process for the separation of carbon nanotubes from graphite
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US5695734A
US5695734AUS08/529,067US52906795AUS5695734AUS 5695734 AUS5695734 AUS 5695734AUS 52906795 AUS52906795 AUS 52906795AUS 5695734 AUS5695734 AUS 5695734A
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metal compound
graphite
carbon nanotubes
metal
mixture
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US08/529,067
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Fumikazu Ikazaki
Kunio Uchida
Motoo Yumura
Satoshi Ohshima
Yasunori Kuriki
Hiroshi Hayakawa
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National Institute of Advanced Industrial Science and Technology AIST
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Abstract

A process for the isolation of carbon nanotubes from a mixture containing carbon nanotubes and graphite is disclosed, which includes the steps of:
(a) reacting the mixture with a metal compound to intercalate the metal compound into the graphite;
(b) reducing the reaction mixture obtained in step (a) to convert the intercalated metal compound to elemental metal;
(c) heating the reduction mixture obtained in step (b) at a temperature of 450-600° C. in an oxygen-containing atmosphere to selectively oxidize the graphite and the elemental metal; and
(d) contacting the heated mixture obtained in step (c) with a liquid to dissolve the oxidized metal in the liquid and to separate the carbon nanotubes as a solid phase from the oxidized metal.

Description

BACKGROUND OF THE INVENTION
This invention relates to a process for the isolation of carbon nanotubes from a mixture containing carbon nanotubes and graphite particles.
Carbon nanotubes are recently discovered, hollow graphite tubules having a diameter of generally several to several tens nanometers. One method for the preparation of carbon nanotubes is disclosed by Ebbesen et al (Nature, 358, 220 (1992)). The crude product obtained by this method contains a large amount of graphite and a small amount of carbon nanotubes. It is thus necessary to separate carbon nanotubes from the graphite.
Ebbesen et al suggest a carbon nanotube separation method in which the crude product is heated at a temperature of 750° C. in an oxidizing atmosphere to selectively burn the graphite and amorphous carbon (Nature, 367, 519 (1994)). Since the amount of the graphite is very large and the difference in oxidizing temperature between the graphite and carbon nanotubes is very small, the known method has a problem in the yield of the carbon nanotubes.
In U.S. Ser. No. 08/283,508, now U.S. Pat. No. 5,560,898 Uchida et al propose a carbon nanotube isolation method in which a mixture containing carbon nanotubes and graphite particles is pulverized, dispersed in a liquid and centrifuged to obtain a precipitate rich in graphite particles and a supernatant containing carbon nanotubes and fine graphite particles. The supernatant is then separated into a solid phase and a liquid phase, and the solid phase is heated in an oxygen-containing atmosphere to selectively burn the graphite particles. This method can separate the carbon nanotubes with an improved yield but requires complicated steps.
SUMMARY OF THE INVENTION
The present invention provides a process for the isolation of carbon nanotubes from a mixture containing carbon nanotubes and graphite, which includes the following steps (a)-(d):
(a) the mixture is reacted with a metal compound to intercalate the metal compound into the graphite, thereby to obtain a reaction mixture containing the carbon nanotubes and the graphite into which the metal compound has been intercalated;
(b) the reaction mixture is reduced to convert the intercalated metal compound to elemental metal, thereby to obtain a reduction mixture containing the carbon nanotubes and the graphite carrying the elemental metal;
(c) the reduction mixture is heated at a temperature of 450°-600° C. in an oxygen-containing atmosphere to selectively oxidize the graphite into CO2 and the elemental metal into a metal oxide, thereby to obtain a heated mixture containing the carbon nanotubes and the metal oxide; and
(d) the heated mixture is contacted with a liquid to dissolve the metal oxide, thereby to separate the carbon nanotubes as a solid phase.
It is the prime object of the present invention to provide a method which can obtain carbon nanotubes with a high purity.
Another object of the present invention is to provide a method which can separate carbon nanotubes from raw material containing graphite and carbon nanotubes at a relatively low temperature.
Other objects, features and advantages of the present invention will become apparent from the detailed description of the invention to follow.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS OF THE INVENTION
In the present invention, a mixture containing carbon nanotubes and graphite is used as a raw material. Such a raw material mixture may be suitably obtained by the method disclosed in the above Ebbesen et al article or by the method disclosed in U.S. Ser. No. 08/372,130 filed Jan. 13, 1995 (Ohshima et al) now U.S. Pat. No. 5,482,601. Generally, the content of the carbon nanotubes in the raw material mixture is at most about 5% by weight. However, the process of the present invention is effective for a raw material mixture having a carbon nanotube content of much more than 5%, for example, 50% by weight.
The raw material mixture is first reacted with a metal compound to intercalate the metal compound between layers of the graphite. The metal compound is preferably a halide. The metal of the metal compound may be, for example, copper, titanium, vanadium, chromium, zinc, molybdenum, tungsten or rhenium. Above all, the use of cupric chloride, or molybdenum chloride is preferred. The intercalation may be performed by heating a blend of the raw material mixture at a temperature of 350°-600° C. in the oxygen-free atmosphere such as under vacuum or in the atmosphere of an inert gas such as nitrogen, argon or helium for a period of time sufficient to effect the intercalation.
It is preferred that the intercalation be carried out in the presence of KCl which serves to lower the fusing point of the reaction mixture. The amount of KCl is generally 0.1-1 part by weight per part by weight of the metal compound. The amount of the metal compound is generally 1-20 parts, preferably 2-10 parts by weight, per part by weight of the raw material mixture containing carbon nanotubes and graphite.
The reaction mixture containing the carbon nanotubes and graphite into which the metal compound has been intercalated is preferably washed with deionized water to remove KCl and unreacted metal compound and is then subjected to a reduction treatment to convert the intercalated metal compound into elemental metal. The reduction treatment may be carried out in a liquid phase by, for example, treating with a reducing agent such as metallic lithium or metallic sodium, in a liquid medium such as a tetrahydrofuran containing naphthalene, or in a gas phase by, for example, treating with a reducing gas such as hydrogen at an elevated temperature of 450°-600° C.
The product obtained by the reduction treatment and containing the carbon nanotubes and the elemental metal-carrying graphite is then oxidized at a temperature of 450°-600° C., preferably 500°-550° C., in an oxidizing atmosphere such as air to selectively burn the graphite. Because of the inclusion of the elemental metal, the graphite may be burnt at a temperature lower than the metal-free graphite, so that the decomposition of the carbon nanotubes may be avoided. By the oxidation treatment, the graphite is converted into carbon dioxide while the elemental metal is converted into the metal oxide.
The product obtained by the above oxidation and containing the carbon nanotubes and metal oxide is treated with a liquid such as an aqueous acid, e.g. hydrochloric acid or nitric acid, to dissolve the metal oxide. By a solid-liquid separation such as by filtration, the carbon nanotubes may be isolated.
The raw material mixture to be treated according to the process of the present invention may additionally contain amorphous carbon. The amorphous carbon is easily decomposed during the oxidizing step and does not adversely affect the purification of carbon nanotubes.
The following examples will further illustrate the present invention.
EXAMPLE 1
Carbon nanotubes were prepared according to the method of Ebessen et al. Two graphite rods were disposed in a carbon cluster producing vessel maintained at a flowing helium pressure of 500 Torr. The anode graphite rod had a diameter of 8 mm. A DC voltage of 18 V was impressed between the two rods. The thus obtained crude carbon nanotube product (1 g) containing carbon nanotubes and graphite was mixed with 4.6 g of cupric chloride and 2.5 g of potassium chloride and the mixture was charged in a glass ampoule under vacuum. The ampoule was closed by fusion and maintained at 400° C. for 7 days so that the cupric chloride was intercalated into the graphite.
The product was then taken out of the ampoule and dispersed in a deionized water, followed by filtration and washing with deionized water. The intercalation product was then heated to 500° C. at a rate of 10° C./minute in the atmosphere of a mixed stream consisting of 50 ml/minute of helium and 50 ml/minute of hydrogen and maintained at that temperature for 1 hour under the same mixed stream so that the cupric chloride was converted into metallic copper.
The reduction product was then heated to 550° C. at a rate of 10° C./minute in air to burn the graphite and to convert metallic copper into cupric oxide. This was dispersed in hydrochloric acid to dissolve cupric oxide, followed by filtration and washing with hydrochloric acid and with water, thereby obtaining solids. The scanning electric microphotograph reveals that the solids are carbon nanotubes containing substantially no graphite.
The invention may be embodied in other specific forms without departing from the spirit or essential characteristics thereof. The present embodiments are therefore to be considered in all respects as illustrative and not restrictive, the scope of the invention being indicated by the appended claims rather than by the foregoing description, and all the changes which come within the meaning and range of equivalency of the claims are therefore intended to be embraced therein.

Claims (16)

What is claimed is:
1. A process for the isolation of carbon nanotubes from a mixture containing carbon nanotubes and graphite, comprising the steps of:
(a) reacting said mixture with a metal compound to intercalate said metal compound into said graphite;
(b) reducing said reaction mixture obtained in step (a) to convert said intercalated metal compound to elemental metal;
(c) heating said reduction mixture obtained in step (b) at a temperature of 450°-600° C. in an oxygen-containing atmosphere to selectively oxidize said graphite and said elemental metal; and
(d) contacting said heated mixture obtained in step (c) with a liquid to dissolve said oxidized metal in said liquid and to separate said carbon nanotubes as a solid phase from said oxidized metal.
2. A process as claimed in claim 1, wherein said metal compound is a metal halide.
3. A process as claimed in claim 1, wherein said metal compound is a metal chloride.
4. A process as claimed in claim 1, wherein step (c) is performed at 500°-550° C.
5. A process as claimed in claim 1, wherein said liquid is an aqueous acid solution.
6. A process as claimed in claim 1 further comprising adding said metal compound and KCl to the mixture prior to step (a).
7. A process as claimed in claim 6 wherein the amount of said KCl added is 0.1-1 part by weight per part by weight of the metal compound.
8. A process as claimed in claim 7 wherein the amount of the metal compound is 1-20 parts by weight per part by weight of said mixture containing carbon nanotubes and graphite.
9. A process as claimed in claim 6 wherein the amount of the metal compound is 1-20 parts by weight per part by weight of said mixture containing carbon nanotubes and graphite.
10. A process as claimed in claim 1 wherein the amount of the metal compound is 1-20 parts by weight per part by weight of said mixture containing carbon nanotubes and graphite.
11. A process as claimed in claim 1 wherein said metal compound is selected from the group consisting of copper, titanium, vanadium, chromium, zinc, molybdenum, tungsten and rhenium.
12. A process as claimed in claim 6 wherein said metal compound is selected from the group consisting of copper, titanium, vanadium, chromium, zinc, molybdenum, tungsten and rhenium.
13. A process as defined in claim 11 wherein said metal compound is a halide.
14. A process as claimed in claim 12 wherein said metal compound is a halide.
15. A process as claimed in claim 11 wherein said metal compound is cupric chloride or molybdenum chloride.
16. A process as claimed in claim 12 wherein said metal compound is cupric chloride or molybdenum chloride.
US08/529,0671994-09-271995-09-15Process for the separation of carbon nanotubes from graphiteExpired - LifetimeUS5695734A (en)

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JP6231222AJP2590442B2 (en)1994-09-271994-09-27 Separation and purification method of carbon nanotube
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US6187823B1 (en)1998-10-022001-02-13University Of Kentucky Research FoundationSolubilizing single-walled carbon nanotubes by direct reaction with amines and alkylaryl amines
US6210800B1 (en)*1996-12-182001-04-03Eidg. Technische Hochschule ZurichUse and production of nanotubes containing a mixed valence venadium
US6331262B1 (en)1998-10-022001-12-18University Of Kentucky Research FoundationMethod of solubilizing shortened single-walled carbon nanotubes in organic solutions
US6333016B1 (en)1999-06-022001-12-25The Board Of Regents Of The University Of OklahomaMethod of producing carbon nanotubes
US6346136B1 (en)*2000-03-312002-02-12Ping ChenProcess for forming metal nanoparticles and fibers
US20020035170A1 (en)*1999-02-122002-03-21Paul GlatkowskiElectromagnetic shielding composite comprising nanotubes
US6368569B1 (en)1998-10-022002-04-09University Of Kentucky Research FoundationMethod of solubilizing unshortened carbon nanotubes in organic solutions
US6413487B1 (en)2000-06-022002-07-02The Board Of Regents Of The University Of OklahomaMethod and apparatus for producing carbon nanotubes
US6451175B1 (en)2000-08-152002-09-17Wisconsin Alumni Research FoundationMethod and apparatus for carbon nanotube production
US20020180077A1 (en)*2001-03-262002-12-05Glatkowski Paul J.Carbon nanotube fiber-reinforced composite structures for EM and lightning strike protection
US20030031620A1 (en)*2001-04-122003-02-13Avetik HarutyunyanPurification of carbon filaments and their use in storing hydrogen
US6531513B2 (en)1998-10-022003-03-11University Of Kentucky Research FoundationMethod of solubilizing carbon nanotubes in organic solutions
US20030175199A1 (en)*2001-09-282003-09-18Iyer Vivekanantan S.Fabrication of carbon nanotube films from alkyne-transition metal complexes
US6641793B2 (en)1998-10-022003-11-04University Of Kentucky Research FoundationMethod of solubilizing single-walled carbon nanotubes in organic solutions
US6740403B2 (en)2001-04-022004-05-25Toyo Tanso Co., Ltd.Graphitic polyhederal crystals in the form of nanotubes, whiskers and nanorods, methods for their production and uses thereof
US20040131532A1 (en)*1999-06-022004-07-08Resasco Daniel E.Method and catalyst for producing single walled carbon nanotubes
US6762237B2 (en)2001-06-082004-07-13Eikos, Inc.Nanocomposite dielectrics
RU2239673C1 (en)*2003-05-072004-11-10Научно-исследовательский институт физики им. В.А. Фока Санкт-Петербургского государственного университетаMethod for isolation of nanotubes from carbon-containing material
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US20050067349A1 (en)*2003-09-252005-03-31Crespi Vincent H.Directed flow method and system for bulk separation of single-walled tubular fullerenes based on helicity
US20050205847A1 (en)*2004-03-172005-09-22Anne DaillyMethods for purifying carbon materials
US20060008406A1 (en)*2004-07-092006-01-12Clean Technologies International CorporationMethod and apparatus for preparing a collection surface for use in producing carbon nanostructures
US20060008405A1 (en)*2004-07-092006-01-12Wagner Anthony SMethod and apparatus for producing carbon nanostructures
US20060008403A1 (en)*2004-07-092006-01-12Clean Technologies International CorporationReactant liquid system for facilitating the production of carbon nanostructures
US20060039848A1 (en)*2004-01-092006-02-23Olga MatarredonaCarbon nanotube pastes and methods of use
US20060057055A1 (en)*2003-12-152006-03-16Resasco Daniel ERhenium catalysts and methods for production of single-walled carbon nanotubes
US20060060825A1 (en)*2001-03-262006-03-23Glatkowski Paul JCoatings comprising carbon nanotubes and methods for forming same
US20060251564A1 (en)*2004-12-312006-11-09Industrial Technology Research InstituteCarbon nanomaterial purification method
US7153903B1 (en)2002-06-192006-12-26The Board Of Regents Of The University Of OklahomaCarbon nanotube-filled composites prepared by in-situ polymerization
US20070116633A1 (en)*2004-07-092007-05-24Clean Technologies International CorporationSpherical carbon nanostructure and method for producing spherical carbon nanostructures
US20070189954A1 (en)*2003-12-302007-08-16Alain PenicaudMethod for dissolving carbon nanotubes and the use thereof
US20090068461A1 (en)*2003-10-162009-03-12The University Of AkronCarbon nanotubes on carbon nanofiber substrate
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US6210800B1 (en)*1996-12-182001-04-03Eidg. Technische Hochschule ZurichUse and production of nanotubes containing a mixed valence venadium
US6605266B2 (en)1996-12-182003-08-12Eidg. Technische Hochschule ZurichUse and process for production of nanotubes
US6531513B2 (en)1998-10-022003-03-11University Of Kentucky Research FoundationMethod of solubilizing carbon nanotubes in organic solutions
US6187823B1 (en)1998-10-022001-02-13University Of Kentucky Research FoundationSolubilizing single-walled carbon nanotubes by direct reaction with amines and alkylaryl amines
US6331262B1 (en)1998-10-022001-12-18University Of Kentucky Research FoundationMethod of solubilizing shortened single-walled carbon nanotubes in organic solutions
US6641793B2 (en)1998-10-022003-11-04University Of Kentucky Research FoundationMethod of solubilizing single-walled carbon nanotubes in organic solutions
US6368569B1 (en)1998-10-022002-04-09University Of Kentucky Research FoundationMethod of solubilizing unshortened carbon nanotubes in organic solutions
US20020035170A1 (en)*1999-02-122002-03-21Paul GlatkowskiElectromagnetic shielding composite comprising nanotubes
US6962892B2 (en)1999-06-022005-11-08The Board Of Regents Of The University Of OklahomaMetallic catalytic particle for producing single-walled carbon nanotubes
US7816709B2 (en)1999-06-022010-10-19The Board Of Regents Of The University Of OklahomaSingle-walled carbon nanotube-ceramic composites and methods of use
US7354881B2 (en)1999-06-022008-04-08The Board Of Regents Of The University Of OklahomaMethod and catalyst for producing single walled carbon nanotubes
US20080107588A1 (en)*1999-06-022008-05-08Resasco Daniel EMethod of producing single-walled carbon nanotubes
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US20070116630A1 (en)*1999-06-022007-05-24Resasco Daniel EMethod of producing single-walled carbon nanotubes
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US6955800B2 (en)2000-06-022005-10-18The Board Of Regents Of The University Of OklahomaMethod and apparatus for producing carbon nanotubes
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US6413487B1 (en)2000-06-022002-07-02The Board Of Regents Of The University Of OklahomaMethod and apparatus for producing carbon nanotubes
US7585482B2 (en)2000-06-022009-09-08The Board Of Regents Of The University Of OklahomaMethod and apparatus for producing carbon nanotubes
US6919064B2 (en)2000-06-022005-07-19The Board Of Regents Of The University Of OklahomaProcess and apparatus for producing single-walled carbon nanotubes
US20080008644A1 (en)*2000-06-022008-01-10Resasco Daniel EMethod and apparatus for producing carbon nanotubes
US20060039849A1 (en)*2000-06-022006-02-23Resasco Daniel EProcess and apparatus for producing single-walled carbon nanotubes
US7459138B2 (en)2000-06-022008-12-02The Board Of Regents Of The University Of OklahomaProcess and apparatus for producing single-walled carbon nanotubes
US20050042162A1 (en)*2000-06-022005-02-24Resasco Daniel E.Process and apparatus for producing single-walled carbon nanotubes
US6451175B1 (en)2000-08-152002-09-17Wisconsin Alumni Research FoundationMethod and apparatus for carbon nanotube production
US20020180077A1 (en)*2001-03-262002-12-05Glatkowski Paul J.Carbon nanotube fiber-reinforced composite structures for EM and lightning strike protection
US6986853B2 (en)2001-03-262006-01-17Eikos, Inc.Carbon nanotube fiber-reinforced composite structures for EM and lightning strike protection
US20060060825A1 (en)*2001-03-262006-03-23Glatkowski Paul JCoatings comprising carbon nanotubes and methods for forming same
US20060078705A1 (en)*2001-03-262006-04-13Glatkowski Paul JCarbon nanotube fiber-reinforced composite structures for EM and lightning strike protection
US7060241B2 (en)2001-03-262006-06-13Eikos, Inc.Coatings comprising carbon nanotubes and methods for forming same
US6740403B2 (en)2001-04-022004-05-25Toyo Tanso Co., Ltd.Graphitic polyhederal crystals in the form of nanotubes, whiskers and nanorods, methods for their production and uses thereof
US20030031620A1 (en)*2001-04-122003-02-13Avetik HarutyunyanPurification of carbon filaments and their use in storing hydrogen
US6869583B2 (en)*2001-04-122005-03-22The Penn State Research FoundationPurification of carbon filaments and their use in storing hydrogen
US6762237B2 (en)2001-06-082004-07-13Eikos, Inc.Nanocomposite dielectrics
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US7357907B2 (en)2001-07-232008-04-15The Board Of Regents Of The University Of OklahomaMethod for producing single walled carbon nanotubes
US7261871B2 (en)*2001-09-282007-08-28The Regents Of The University Of CaliforniaFabrication of carbon nanotube films from alkyne-transition metal complexes
US20030175199A1 (en)*2001-09-282003-09-18Iyer Vivekanantan S.Fabrication of carbon nanotube films from alkyne-transition metal complexes
US20100160553A1 (en)*2002-06-192010-06-24Mcdaniel Neal DMethods of making polymer composites containing single-walled carbon nanotubes
US7153903B1 (en)2002-06-192006-12-26The Board Of Regents Of The University Of OklahomaCarbon nanotube-filled composites prepared by in-situ polymerization
US20070004857A1 (en)*2002-06-192007-01-04Barraza Harry JCarbon nanotube-filled composites prepared by in-situ polymerization
US7829622B2 (en)2002-06-192010-11-09The Board Of Regents Of The University Of OklahomaMethods of making polymer composites containing single-walled carbon nanotubes
RU2239673C1 (en)*2003-05-072004-11-10Научно-исследовательский институт физики им. В.А. Фока Санкт-Петербургского государственного университетаMethod for isolation of nanotubes from carbon-containing material
US20050067349A1 (en)*2003-09-252005-03-31Crespi Vincent H.Directed flow method and system for bulk separation of single-walled tubular fullerenes based on helicity
US7347981B2 (en)2003-09-252008-03-25The Penn State Research FoundationDirected flow method and system for bulk separation of single-walled tubular fullerenes based on helicity
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